Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1165292818 | 11652928 | 18 | F | 2015 | 20160823 | 20151022 | 20160829 | EXP | CA-PFIZER INC-2015283489 | PFIZER | 52.00 | YR | F | Y | 0.00000 | 20160829 | MD | CA | CA |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1165292818 | 11652928 | 1 | PS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | 203214 | 5 | MG | TABLET | BID | ||||||
1165292818 | 11652928 | 2 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | 203214 | 5 | MG | TABLET | BID | ||||||
1165292818 | 11652928 | 3 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | 203214 | 5 | MG | TABLET | BID | ||||||
1165292818 | 11652928 | 4 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 15 MG, WEEKLY | 11719 | 15 | MG | /wk | |||||||
1165292818 | 11652928 | 5 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 15 MG, WEEKLY | 11719 | 15 | MG | /wk | |||||||
1165292818 | 11652928 | 6 | SS | NAPROSYN | NAPROXEN | 1 | UNK | 0 | |||||||||||
1165292818 | 11652928 | 7 | SS | NAPROSYN | NAPROXEN | 1 | 2X/DAY | 0 | BID | ||||||||||
1165292818 | 11652928 | 8 | SS | ATASOL | ACETAMINOPHEN | 1 | UNK, AS NEEDED | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
1165292818 | 11652928 | 1 | Rheumatoid arthritis |
1165292818 | 11652928 | 4 | Rheumatoid arthritis |
1165292818 | 11652928 | 6 | Pain |
1165292818 | 11652928 | 8 | Pain |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
1165292818 | 11652928 | HO |
1165292818 | 11652928 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
1165292818 | 11652928 | Abdominal pain | |
1165292818 | 11652928 | Chromaturia | |
1165292818 | 11652928 | Condition aggravated | |
1165292818 | 11652928 | Diarrhoea | |
1165292818 | 11652928 | Drug effect incomplete | |
1165292818 | 11652928 | Dysuria | |
1165292818 | 11652928 | Eye pain | |
1165292818 | 11652928 | Fatigue | |
1165292818 | 11652928 | Haemorrhoids | |
1165292818 | 11652928 | Incontinence | |
1165292818 | 11652928 | Nail bed bleeding | |
1165292818 | 11652928 | Nail infection | |
1165292818 | 11652928 | Nasopharyngitis | |
1165292818 | 11652928 | Pain in extremity | |
1165292818 | 11652928 | Peripheral swelling | |
1165292818 | 11652928 | Pollakiuria | |
1165292818 | 11652928 | Pyrexia | |
1165292818 | 11652928 | Urinary retention | |
1165292818 | 11652928 | Uterine cancer | |
1165292818 | 11652928 | Vaginal infection | |
1165292818 | 11652928 | Vision blurred |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
1165292818 | 11652928 | 1 | 20150821 | 20151104 | 0 | |
1165292818 | 11652928 | 2 | 20151109 | 20160315 | 0 | |
1165292818 | 11652928 | 3 | 2016 | 0 | ||
1165292818 | 11652928 | 4 | 20160308 | 0 | ||
1165292818 | 11652928 | 5 | 2016 | 0 |